(Q37765824)

22 August 2017

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title

Gene polymorphisms and their role in epilepsy treatment and prognosis (English)

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22 August 2017

Ortrud K Steinlein

1

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22 August 2017

language of work or name

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16 June 2010

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Naunyn-Schmiedeberg's Archives of Pharmacology

22 August 2017

published in

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22 August 2017

volume

382

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22 August 2017

issue

2

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22 August 2017

page(s)

109-118

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Major malformations in offspring of women with epilepsy

22 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00210-010-0531-8

Influence of the MTHFR genotype on the rate of malformations following exposure to antiepileptic drugs in utero

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00210-010-0531-8

TNFalpha promoter region gene polymorphisms in carbamazepine-hypersensitive patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00210-010-0531-8

Endoplasmic reticulum stress and apoptosis signaling in human temporal lobe epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00210-010-0531-8

Genome-wide linkage scan for loci associated with epilepsy in Belgian shepherd dogs

21 January 2018

1 reference

12 December 2020

ABCC2 haplotype is not associated with drug-resistant epilepsy.

1 reference

12 December 2020

Antiepileptic drug-induced hypersensitivity syndrome reactions

1 reference

12 December 2020

Genetic factors associated with drug-resistance of epilepsy: relevance of stratification by patient age and aetiology of epilepsy

1 reference

12 December 2020

Adenosine A2A receptor deficient mice are partially resistant to limbic seizures

1 reference

12 December 2020

Isobolographic characterization of interactions of retigabine with carbamazepine, lamotrigine, and valproate in the mouse maximal electroshock-induced seizure model.

1 reference

12 December 2020

The autosomal recessively inherited progressive myoclonus epilepsies and their genes

1 reference

12 December 2020

Serious carbamazepine-induced hypersensitivity reactions associated with the HSP70 gene cluster

1 reference

12 December 2020

Haplotype structure of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene and its relationship to serum total bilirubin concentration in a male Korean population.

1 reference

12 December 2020

Involvement of multiple UDP-glucuronosyltransferase 1A isoforms in glucuronidation of 5-(4'-hydroxyphenyl)-5-phenylhydantoin in human liver microsomes

1 reference

12 December 2020

Neuronal nicotinic receptors and epilepsy, from genes to possible therapeutic compounds

1 reference

12 December 2020

The role of pharmacogenetics in the metabolism of antiepileptic drugs: pharmacokinetic and therapeutic implications

1 reference

12 December 2020

Comparison of phenytoin with noncompetitive N-methyl-D-aspartate antagonists in a model of focal brain ischemia in rat.

1 reference

12 December 2020

Mechanisms of action of antiepileptic drugs: the search for synergy

1 reference

12 December 2020

Polymorphisms in genes related to folate and cobalamin metabolism and the associations with complex birth defects

1 reference

12 December 2020

Pleiotropic functional effects of the first epilepsy-associated mutation in the human CHRNA2 gene

1 reference

12 December 2020

Epilepsy pharmacogenetics

1 reference

12 December 2020

Human disorders caused by the disruption of the regulation of excitatory neurotransmission

1 reference

12 December 2020

Molecular background of progressive myoclonus epilepsy

1 reference

12 December 2020

Silent SNPs: impact on gene function and phenotype

1 reference

12 December 2020

Polymorphism of the MDR1/ABCB1 C3435T drug-transporter and resistance to anticonvulsant drugs: a meta-analysis

1 reference

12 December 2020

Adrenocorticotropic hormone versus pulsatile dexamethasone in the treatment of infantile epilepsy syndromes

1 reference

12 December 2020

Genetic polymorphisms in the TATA box and upstream phenobarbital-responsive enhancer module of the UGT1A1 promoter have combined effects on UDP-glucuronosyltransferase 1A1 transcription mediated by constitutive androstane receptor, pregnane X recept

1 reference

12 December 2020

ABCB1 polymorphisms influence the response to antiepileptic drugs in Japanese epilepsy patients

1 reference

12 December 2020

UDP-glucuronosyltransferases: gene structures of UGT1 and UGT2 families

1 reference

12 December 2020

Transcriptional activation of PPARalpha by phenobarbital in the absence of CAR and PXR.

1 reference

12 December 2020

Concordance of primary generalised epilepsy and carbamazepine hypersensitivity in monozygotic twins

1 reference

12 December 2020

Medical genetics: a marker for Stevens-Johnson syndrome

1 reference

12 December 2020

The state of the art in the genetic analysis of the epilepsies

1 reference

12 December 2020

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

1 reference

12 December 2020

CYP2C9*1B promoter polymorphisms, in linkage with CYP2C19*2, affect phenytoin autoinduction of clearance and maintenance dose

1 reference

12 December 2020

Leader of the pack: gene mapping in dogs and other model organisms

1 reference

12 December 2020

Fetal anticonvulsant syndrome and mutation in the maternal MTHFR gene

1 reference

12 December 2020

A pharmacogenetic exploration of vigabatrin-induced visual field constriction

1 reference

12 December 2020

Mechanisms of action of antiepileptic drugs

1 reference

12 December 2020

Carbamazepine-induced drug-induced hypersensitivity syndrome in a 14-year-old Japanese boy.

1 reference

12 December 2020

Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene

1 reference

12 December 2020

Reversible valproate hepatotoxicity due to mutations in mitochondrial DNA polymerase gamma (POLG1).

1 reference

12 December 2020

The effects of genetic polymorphisms of CYP2C9 and CYP2C19 on phenytoin metabolism in Japanese adult patients with epilepsy: studies in stereoselective hydroxylation and population pharmacokinetics

1 reference

12 December 2020

Clinical significance of animal seizure models and mechanism of action studies of potential antiepileptic drugs

1 reference

12 December 2020

RNA dust: where are the genes?

1 reference

12 December 2020

Fetal anticonvulsant syndromes and polymorphisms in MTHFR, MTR, and MTRR.

1 reference

12 December 2020

Genetics of human neural tube defects

1 reference

12 December 2020

Lack of association between ABCB1, ABCG2, and ABCC2 genetic polymorphisms and multidrug resistance in partial epilepsy

1 reference

12 December 2020

The longer term outcome of children born to mothers with epilepsy

1 reference

12 December 2020

An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy

1 reference

12 December 2020

ACTH receptor (MC2R) promoter variants associated with infantile spasms modulate MC2R expression and responsiveness to ACTH.

1 reference

12 December 2020

Congenital malformations due to antiepileptic drugs

1 reference

12 December 2020

The history of barbiturates a century after their clinical introduction

1 reference

12 December 2020

Association between HLA-B*1502 allele and antiepileptic drug-induced cutaneous reactions in Han Chinese

1 reference

12 December 2020

Mutated nicotinic receptors responsible for autosomal dominant nocturnal frontal lobe epilepsy are more sensitive to carbamazepine

1 reference

12 December 2020

Genetic basis for idiosyncratic reactions to antiepileptic drugs

1 reference

12 December 2020

Association of Multidrug Resistance in Epilepsy with a Polymorphism in the Drug-Transporter GeneABCB1

1 reference

12 December 2020

Pathobiology and genetics of neural tube defects.

1 reference

12 December 2020

Toxic epidermal necrolysis as a dermatological manifestation of drug hypersensitivity syndrome

1 reference

12 December 2020

Management of epilepsy with diphenylhydantoin sodium. Dosage regulation for problem patients

1 reference

12 December 2020

Properties of neuronal nicotinic acetylcholine receptor mutants from humans suffering from autosomal dominant nocturnal frontal lobe epilepsy

1 reference

12 December 2020

Transcriptional regulation of human UGT1A1 gene expression through distal and proximal promoter motifs: implication of defects in the UGT1A1 gene promoter

1 reference

12 December 2020

Study of the genetic determinants of UGT1A1 inducibility by phenobarbital in cultured human hepatocytes

1 reference

12 December 2020

Reversible lamotrigine-induced neurobehavioral disturbances in children with epilepsy

1 reference

12 December 2020

The multimodal prospects for neuroprotection and disease modification in epilepsy: relationship to its challenging neurobiology.

1 reference

12 December 2020

Modulation of UDP-glucuronosyltransferase 1A1 in primary human hepatocytes by prototypical inducers

1 reference

12 December 2020

Phenytoin toxicity due to genetic polymorphism

1 reference

12 December 2020

Expanded repeat in canine epilepsy

1 reference

12 December 2020

Hierarchical regulation of mitochondrion-dependent apoptosis by BCL-2 subfamilies

1 reference

12 December 2020

Antiepileptic drug use of women with epilepsy and congenital malformations in offspring

1 reference

12 December 2020

Tramadol-induced seizurogenic effect: a possible role of opioid-dependent histamine H1 receptor activation-linked mechanism

1 reference

12 December 2020

A European study of HLA-B in Stevens-Johnson syndrome and toxic epidermal necrolysis related to five high-risk drugs

1 reference

12 December 2020

The phenobarbital response enhancer module in the human bilirubin UDP-glucuronosyltransferase UGT1A1 gene and regulation by the nuclear receptor CAR.

1 reference

12 December 2020

Valproic acid aggravates epilepsy due to MELAS in a patient with an A3243G mutation of mitochondrial DNA.

1 reference

12 December 2020

Non–coding RNA genes and the modern RNA world

1 reference

12 December 2020

Association between ABCB1 C3435T polymorphism and drug-resistant epilepsy in Han Chinese

1 reference

12 December 2020

Genetic factors in seizures: a population-based study of 47,626 US, Norwegian and Danish twin pairs.

1 reference

12 December 2020

A high frequency of the MTHFR 677C>T polymorphism in Scottish women with epilepsy: possible role in pathogenesis

1 reference

12 December 2020

Tobacco habits modulate autosomal dominant nocturnal frontal lobe epilepsy

1 reference

12 December 2020

Bcl-w protects hippocampus during experimental status epilepticus.

1 reference

12 December 2020

Non-response to antiepileptic pharmacotherapy is associated with the ABCC2 -24C>T polymorphism in young and adult patients with epilepsy.

1 reference

12 December 2020

Initial sequencing and analysis of the human genome

1 reference

12 December 2020

Brain pseudoatrophy and mental regression on valproate and a mitochondrial DNA mutation

1 reference

12 December 2020

10.1007/S00210-010-0531-8

Identifiers

DOI

1 reference

release_7hvj66x7yvdbbofx5j6sn4nn3a

22 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/7hvj66x7yvdbbofx5j6sn4nn3a

24 November 2022

mapped directly with Wikidata item

1 reference